EXPEDIUM VERSE 199723550SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034443331), received between Nov 10, 2020 and Nov 10, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 10, 2020Break; Break

  DEVICE REPORT FROM (B)(6) REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2020, WHILE INSERTING THE NUT, JUST PAST THE WING OF THE VERSE SCREW, THE NUT BEGAN TO FILLET. ANOTHER NUT WAS TRIED WITHOUT SUCCESS. THIS HAPPENED ON THREE (3) SCREWS, WHICH HAD TO BE REPLACED. ONE OF THE SCREWS WAS INSERTED WITH A LARGER DIAMETER. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A 120 MINUTE DELAY. THIS REPORT IS FOR ONE (1) EXPEDIUM VERSE SPINE SYSTEM FENESTRATED CORTICAL FIX POLYAXIAL SCREW 5.0 X 50MM. THIS IS REPORT 2 OF 3 FOR (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10817598 ↗